Case Report: Late-onset primary hemophagocytic lymphohistiocytosis leading to the diagnosis of Griscelli syndrome type 2 in a young woman with phenotypically inapparent partial albinism
病例报告：一名表型不明显的年轻女性，因迟发性原发性噬血细胞性淋巴组织细胞增生症确诊为格里塞利综合征2型。
期刊:Frontiers in Immunology
影响因子:5.9
doi:10.3389/fimmu.2025.1604460
Rausch, Johanna; Herold, Stephanie; Liebhäuser, Simone; Bülbül, Yagmur; Antunes Ferreira, Edite; Wenz, Till; Legscha, Kevin Jan; Bros, Matthias; Butsch, Florian; Kriege, Oliver; Warnatz, Klaus; Groß, Miriam; Lehmberg, Kai; Lichtenfeld, Helena Clara; La Rosée, Paul; Radsak, Markus Philipp; Theobald, Matthias; Echchannaoui, Hakim; Munder, Markus
